'Click synthesis' of some novel o-substituted oximes containing 1,2,3-triazole-1,4-diyl residues as new analogs of β-adrenoceptor antagonists

Helvetica Chimica Acta

Volumn 95, Issue 3, 2012, Pages 491-501

  Rad, Mohammad Navid Soltani ^a   Behrouz, Somayeh ^a   Karimitabar, Fatemeh ^b   Khalafi Nezhad, Ali ^b  

^a SHIRAZ UNIVERSITY OF TECHNOLOGY   (Iran)

^b SHIRAZ UNIVERSITY   (Iran)

Author keywords

Adrenoceptor antagonist; 'Click synthesis'; Huisgen cycloaddition; O Oxime ethers

Indexed keywords

'CLICK SYNTHESIS'; GOOD YIELD; HUISGEN CYCLOADDITION; PROPARGYL BROMIDES; TARGET COMPOUND;

BROMINE COMPOUNDS; ETHERS;

SYNTHESIS (CHEMICAL);

1,2,3 TRIAZOLE 1,4 DIYL DERIVATIVE; 9H FLUOREN 9 ONE; 9H FLUOREN 9 ONE O [[1 (2 HYDROXY 3 PHENOXYPROPYL) 1H 1,2,3 TRIAZOL 4 YL]METHYL]OXIME; 9H FLUOREN 9 ONE O [[1 (2 HYDROXYBUTYL) 1H 1,2,3 TRIAZOL 4 YL]METHYL]OXIME; 9H FLUOREN 9 ONE O [[1 (2 HYDROXYCYCLOHEXYL) 1H 1,2,3 TRIAZOL 4 YL]METHYL]OXIME; 9H FLUOREN 9 ONE O [[1 (3 BUTOXY 2 HYDROXYPROPYL) 1H 1,2,3 TRIAZOL 4 YL]METHYL]OXIME; 9H FLUOREN 9 ONE O [[1 [2 HYDROXY 3 (4 METHOXYPHENOXY)PROPYL] 1H 1,2,3 TRIAZOL 4 YL]METHYL]OXIME; 9H FLUOREN 9 ONE O [[1 [2 HYDROXY 3 (NAPHTHALEN 2 YLOXY)PROPYL] 1H 1,2,3 TRIAZOL 4 YL]METHYL]OXIME; 9H FLUOREN 9 ONE O [[1 [2 HYDROXY 3 (PROP 2 EN 1 YLOXY)PROPYL] 1H 1,2,3 TRIAZOL 4 YL]METHYL]OXIME; 9H FLUOREN 9 ONE O [[1 [2 HYDROXY 3 [4 (PHENYLMETHYL)PHENOXY]PROPYL] 1H 1,2,3 TRIAZOL 4 YL]METHYL]OXIME; 9H FLUOREN 9 ONE O [[1 [3 (2,4 DICHLOROPHENOXY) 2 HYDROXYPROPYL] 1H 1,2,3 TRIAZOL 4 YL]METHYL]OXIME; 9H FLUOREN 9 ONE O [[1 [3 (4 CHLOROPHENOXY) 2 HYDROXYPROPYL] 1H 1,2,3 TRIAZOL 4 YL]METHYL]OXIME; BENZOPHENONE; BETA ADRENERGIC RECEPTOR BLOCKING AGENT; DIPHENYLMETHANONE O [[1 (2 HYDROXY 3 PHENOXYPROPYL) 1H 1,2,3 TRIAZOL 4 YL]METHYL]OXIME; DIPHENYLMETHANONE O [[1 (2 HYDROXYBUTYL) 1H 1,2,3 TRIAZOL 4 YL]METHYL]OXIME; DIPHENYLMETHANONE O [[1 (2 HYDROXYCYCLOHEXYL) 1H 1,2,3 TRIAZOL 4 YL]METHYL]OXIME; DIPHENYLMETHANONE O [[1 (3 BUTOXY 2 HYDROXYPROPYL) 1H 1,2,3 TRIAZOL 4 YL]METHYL]OXIME; DIPHENYLMETHANONE O [[1 [2 HYDROXY 3 (4 METHOXYPHENOXY)PROPYL] 1H 1,2,3 TRIAZOL 4 YL]METHYL]OXIME; DIPHENYLMETHANONE O [[1 [2 HYDROXY 3 (NAPHTHALEN 2 YLOXY)PROPYL] 1H 1,2,3 TRIAZOL 4 YL]METHYL]OXIME; DIPHENYLMETHANONE O [[1 [2 HYDROXY 3 (PROP 2 EN 1 YLOXY)PROPYL] 1H 1,2,3 TRIAZOL 4 YL]METHYL]OXIME; DIPHENYLMETHANONE O [[1 [2 HYDROXY 3 [4 (PHENYLMETHYL)PHENOXY]PROPYL] 1H 1,2,3 TRIAZOL 4 YL]METHYL]OXIME; DIPHENYLMETHANONE O [[1 [3 (2,4 DICHLOROPHENOXY) 2 HYDROXYPROPYL] 1H 1,2,3 TRIAZOL 4 YL]METHYL]OXIME; DIPHENYLMETHANONE O [[1 [3 (4 CHLOROPHENOXY) 2 HYDROXYPROPYL] 1H 1,2,3 TRIAZOL 4 YL]METHYL]OXIME; O PROPARGYL OXIME DERIVATIVE; PROPARGYL BROMIDE; UNCLASSIFIED DRUG;

ARTICLE; CATALYSIS; CYCLOADDITION; DRUG STRUCTURE; DRUG SYNTHESIS; PRIORITY JOURNAL;

EID: 84859056347     PISSN: 0018019X     EISSN: 15222675     Source Type: Journal    
DOI: 10.1002/hlca.201100324     Document Type: Article

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